PHOX2B NM_003924.4(PHOX2B):c.753_767del (p.Ala256_Ala260del) — variant · CancerIndex

Variant · Deletion

PHOX2B NM_003924.4(PHOX2B):c.753_767del (p.Ala256_Ala260del)

CI-VAR-00073632Explore in graph →p.Ala256_Ala260delNM_003924.4:c.753_767delClinVar 467742 rs779557320

Curated evidence

Evidence by cancer (0 items)

Grouped by cancer context first, then therapy. The same variant can be sensitizing in one cancer and irrelevant in another — contexts are never merged. 50 items per page; a cancer group may continue on the next page.

Data not yet available

No curated evidence item references this variant yet.

ClinVar

Clinical significance (1)

ClinVar interpretations are shown as structured records — significance, review status, star rating, conditions — never flattened into one word.

clinvarCurated1 interpretation · review status and star rating as assigned by ClinVar.

Variation	Clinical significance	Review status	Stars	Conditions	Origin	Submitters	Last evaluated	Source
467742	Likely benign	criteria provided, multiple submitters, no conflicts	2	Haddad syndrome; Hereditary cancer-predisposing syndrome; PHOX2B-related disorder	germline	4	Nov 17, 2025	clinvar